芬苯达唑超分子复合物对胚胎发育影响的评价

A. I. Varlamova, N. B. Emelyanova, I. Arkhipov, T. S. Novik, K. Kurochkina, V. Abramov
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引用次数: 0

摘要

本研究的目的是研究苯咪唑超分子配合物(SMСF)的促胚作用。材料和方法。根据新药理学物质的实验(临床前)研究指南,在40只白色雌性大鼠和20只雄性大鼠身上进行了评估SMCF胚胎性特性的实验。将怀孕雌性大鼠分为3个实验组和1个对照组。SMCF在胚胎发生的1-6天灌胃给药(第1组);在第7-14天(第2组)和第15-19天(第3组),以3倍治疗剂量-6.0 mg/kg的活性物质。对照组的动物从怀孕的第一天到第19天接受生理盐水。大鼠在妊娠第20天被实施安乐死。剖腹手术后取出带胎儿的子宫,记录黄体数量、植入部位、活胎、死胎和吸收胎的数量,测定胎盘的重量和直径。对胚胎进行检查、称重,确定头尾大小,计算胚胎总死亡、植入前和植入后胚胎死亡的水平。根据J.G.Wilson(1965)和A.B.Dawson(1926)的方法对胎儿进行内脏异常和骨骼系统变化检查,该方法在苏联医学科学院胚胎学系进行了修改。结果和讨论。因此,SMCF不会对胎儿产生毒性影响:1-6日灌胃给予6,0 mg/kg的三倍治疗剂量时,胚胎的死亡率、大小和重量与对照组持平;妊娠7-14天和15-19天。SMCF未引起内外畸形。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of supramolecular complex of fenbendazole effect on embryonic development
The purpose of the research is to study the embryotropic effect of supramolecular complex of fenbendazole (SMСF).Materials and methods. The experiment to assess the embryotropic properties of SMCF was carried out on 40 white female and 20 male rats in accordance with the Guidelines for the experimental (preclinical) study of new pharmacological substances. Pregnant female rats were divided into 3 experimental and one control groups. SMCF was administered intragastrically on the 1–6 days of embryogenesis (group 1); on the 7–14 days (group 2) and on the 15–19 days (group 3) in three times therapeutic dose – 6,0 mg/kg of active substance. The animals of the control group received saline from the first to the 19th days of pregnancy. Rats were euthanized on the 20th day of pregnancy. The uterus with fetuses was removed after laparotomy, the number of corpora lutea, implantation sites, the number of living, dead and resorbed fetuses were recorded, the weight and diameter of the placenta were determined. The embryos were examined, weighed, the craniocaudal sizes were determined, the levels of total embryonic, preimplantation and postimplantation embryo death were calculated. The fetuses were examined for abnormalities of internal organs and changes in the skeletal system according to the methods of J. G. Wilson (1965) and A. B. Dawson (1926), modified in the department of embryology of the IEM of the USSR Academy of Medical Sciences.Results and discussion. As a result, SMCF does not induce toxic effects on the fetus: mortality rates, size and weight of embryos were at the level of the control group in a threefold therapeutic dose 6,0 mg/kg at intragastric administration on the 1–6; 7–14 and 15–19 days of pregnancy. SMCF did not cause external and internal malformations.
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